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- source_evidence_literature type ECO_0000212 NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.
- NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_assertion description "[These results suggest that GYLTL1B may be a candidate gene for muscular dystrophy and that its overexpression could compensate for the deficiency of both LARGE and other glycosyltransferases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.
- NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_assertion evidence source_evidence_literature NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.
- NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_assertion SIO_000772 15661757 NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.
- NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_assertion wasDerivedFrom befree-2016 NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.
- NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_assertion wasGeneratedBy ECO_0000203 NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.
- befree-2016 importedOn "2016-02-19" NP477158.RAtDDgj97iQcdThbBmOtFxog1sw3507ZqdCRxaTpSio0c130_provenance.